“…1,2 Although many different enzymes and substrates have been used in ERMs, most of these rely on bond formation or cleavage reactions that primarily employ proteases, nucleases, or kinases/phosphatases. Many ERMs also utilize specific peptide or oligonucleotide sequences as enzyme substrates, 1,2 which in turn increases the cost and complexity of ERM preparation. To enable widespread use of ERMs in various applications, such as diagnostics, sensors, drug delivery, adaptive surfaces, and regenerative medicine, it would be advantageous to be able to create ERMs that respond to different classes of enzymatic reactions, and that can be prepared using atom economical, scalable methods.…”